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13752-84-6

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13752-84-6 Usage

General Description

2,3,4-trihydroxybutanoic acid, also known as trihydroxybutyric acid, is a organic compound with the molecular formula C4H8O5. It is a colorless solid that occurs naturally in many fruits and vegetables, including grapes, wine, and beer. It is a member of the beta-hydroxy acid family, and its chemical structure features three hydroxyl (OH) groups attached to a butyric acid base. 2,3,4-trihydroxybutanoic acid is widely used in the food and pharmaceutical industries as a flavor enhancer, acidulant, and chelating agent due to its tart taste and ability to bind to metal ions. Additionally, 2,3,4-trihydroxybutanoic acid is a key intermediate in the biosynthesis of certain amino acids and fatty acids in living organisms.

Check Digit Verification of cas no

The CAS Registry Mumber 13752-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,5 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13752-84:
(7*1)+(6*3)+(5*7)+(4*5)+(3*2)+(2*8)+(1*4)=106
106 % 10 = 6
So 13752-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O5/c5-1-2(6)3(7)4(8)9/h2-3,5-7H,1H2,(H,8,9)/t2-,3-/m1/s1

13752-84-6Relevant articles and documents

Glattfeld,Kribben

, p. 1720,1723 (1939)

KINETICS AND MECHANISM OF Ru(III) CATALYSED OXYDATION OF SOME POLYHYDRIC ALCOHOLS BY N-BROMOSUCCINIMIDE IN ACIDIC MEDIA

Sharma, J. P.,Singh, R. N. P.,Singh, A. K.,Singh, Bharat

, p. 2739 - 2748 (2007/10/02)

Kinetics of oxydation of ethylene glycol, glycerol, erythritol and dulcitol by acidic solution of N-bromosuccinimide (NBS) in presence of ruthenium(III) chloride as a homogeneous catalyst and mercuric acetate as scavenger in the temperature range of 30-50 deg C have been reported.The reactions follow identical kinetics, being first order in each NBS, substrate and Ru(III).Zero effect of , and ionic strength has been observed.A negative effect of succinimide and acetic acid is observed while shows the positive effect on reaction velocity.Various activation parameters have been computed.The products of the reaction were identified as the corresponding acids.A suitable mechanism consistent with the experimental results has been proposed.

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